Partial ADAMTS13 deficiency in atypical hemolytic uremic syndrome.
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Complement factor B mutations in atypical hemolytic uremic syndrome-disease-relevant or benign?Successful Remission of Hemolytic-Uremic Syndrome During the Third-line Weekly Gemcitabine for Metastatic Breast CancerClass II human leucocyte antigen DRB1*11 in hairy cell leukaemia patients with and without haemolytic uraemic syndrome.Absolute immature platelet count dynamics in diagnosing and monitoring the clinical course of thrombotic thrombocytopenic purpura.Identification and management of atypical hemolytic uremic syndrome immediately post-heart transplantation.An international consensus approach to the management of atypical hemolytic uremic syndrome in children.Modified Ham test for atypical hemolytic uremic syndromeRole of the skin biopsy in the diagnosis of atypical hemolytic uremic syndrome.Variable Eculizumab Clearance Requires Pharmacodynamic Monitoring to Optimize Therapy for Thrombotic Microangiopathy after Hematopoietic Stem Cell Transplantation.The genetic fingerprint of susceptibility for transplant-associated thrombotic microangiopathy.von Willebrand factor is a cofactor in complement regulation.Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patientsReincarnation of ancient links between coagulation and complement.Rationale for Adjunctive Therapies for Pediatric Sepsis Induced Multiple Organ Failure.Acquired thrombotic thrombocytopenic purpura and atypical hemolytic uremic syndrome successfully treated with eculizumab.Factors influencing treatment of atypical hemolytic uremic syndrome.ADAMTS13 missense variants associated with defective activity and secretion of ADAMTS13 in a patient with non-cirrhotic portal hypertension.Targeted exome sequencing in anti-factor H antibody negative HUS reveals multiple variations.The role of von Willebrand factor in thrombotic microangiopathy.Thrombocytopenia in the ICU: disseminated intravascular coagulation and thrombotic microangiopathies-what intensivists need to know.Thrombotic thrombocytopenic purpuraGemcitabine-induced haemolytic uremic syndrome, although infrequent, can it be prevented: A case report and review of literatureTTP-like syndrome: novel concept and molecular pathogenesis of endotheliopathy-associated vascular microthrombotic disease
P2860
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P2860
Partial ADAMTS13 deficiency in atypical hemolytic uremic syndrome.
description
2013 nî lūn-bûn
@nan
2013 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Partial ADAMTS13 deficiency in atypical hemolytic uremic syndrome.
@ast
Partial ADAMTS13 deficiency in atypical hemolytic uremic syndrome.
@en
type
label
Partial ADAMTS13 deficiency in atypical hemolytic uremic syndrome.
@ast
Partial ADAMTS13 deficiency in atypical hemolytic uremic syndrome.
@en
prefLabel
Partial ADAMTS13 deficiency in atypical hemolytic uremic syndrome.
@ast
Partial ADAMTS13 deficiency in atypical hemolytic uremic syndrome.
@en
P2093
P2860
P1433
P1476
Partial ADAMTS13 deficiency in atypical hemolytic uremic syndrome.
@en
P2093
Carla M Nester
Michael H Kroll
Richard J Smith
Shuju Feng
Stephen J Eyler
Vahid Afshar-Kharghan
Yuzhou Zhang
P2860
P304
P356
10.1182/BLOOD-2013-03-492421
P407
P577
2013-07-11T00:00:00Z